JP2003293022A - Method for producing molten low nitrogen and chromium- containing steel - Google Patents

Method for producing molten low nitrogen and chromium- containing steel

Info

Publication number
JP2003293022A
JP2003293022A JP2002098202A JP2002098202A JP2003293022A JP 2003293022 A JP2003293022 A JP 2003293022A JP 2002098202 A JP2002098202 A JP 2002098202A JP 2002098202 A JP2002098202 A JP 2002098202A JP 2003293022 A JP2003293022 A JP 2003293022A
Authority
JP
Japan
Prior art keywords
chromium
molten steel
producing
slag
ladle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2002098202A
Other languages
Japanese (ja)
Other versions
JP3774674B2 (en
Inventor
Kenji Hiyoshi
研二 日吉
Munechika Nishitani
宗親 西谷
Tomoyuki Imamura
智之 今村
Noboru Takatsuka
昇 高塚
Ryuzo Hayakawa
隆造 早川
Ryo Watanabe
涼 渡邊
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP2002098202A priority Critical patent/JP3774674B2/en
Publication of JP2003293022A publication Critical patent/JP2003293022A/en
Application granted granted Critical
Publication of JP3774674B2 publication Critical patent/JP3774674B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Treatment Of Steel In Its Molten State (AREA)
  • Carbon Steel Or Casting Steel Manufacturing (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing molten low nitrogen and chromium-containing steel by which molten low nitrogen and high purity chromium-containing steel is provided by reducing a degassing treatment in a reduced-pressure secondary decarburization-refining process and the shortening of a treating time in a reduced-pressure secondary decarburization-refining furnace, the reduction of a refractory cost, etc., can be obtained. <P>SOLUTION: A reduction-treatment of chromium oxide in slag is applied by dividedly adding CO<SB>2</SB>generating material 13 after adding a reduced agent into the molten chromium-containing steel performing the decarburization- refining in a converter 1. Successively, the reduced-pressure secondary decarburization-refining is applied after tapping off the chromium-containing steel 8 performing the reduction treatment in a ladle 12 charging the CO<SB>2</SB>generating material 13. <P>COPYRIGHT: (C)2004,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、転炉及び減圧二次
脱炭精錬炉を用いて窒素含有量の少ない含クロム溶鋼を
溶製する低窒素含クロム溶鋼の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a low nitrogen chromium-containing molten steel, which comprises melting a chromium-containing molten steel having a low nitrogen content using a converter and a reduced pressure secondary decarburizing / refining furnace.

【0002】[0002]

【従来の技術】従来、含クロム溶鋼は、上底吹き転炉及
び上吹き転炉等の転炉型の脱炭精錬炉を用いて炭素濃度
が0.3〜1.0質量%に脱炭した粗溶鋼を溶製した
後、この粗溶鋼を取鍋に出鋼する。そして、この取鍋を
用いた減圧二次脱炭精錬処理で、昇熱用のAl合金を添
加した後、吹酸して粗溶鋼の昇熱と二次脱炭精錬を行っ
てから含クロム溶鋼を溶製している。更に、近年では、
含クロム溶鋼の加工性を高めるため、低窒素(低N)化
を指向する鋼種が増加しており、転炉での低N化を行っ
ているが十分でなく、減圧二次脱炭精錬処理工程の吹酸
脱炭精錬の途中で、脱ガス処理を行うことを余儀なくさ
れており、減圧二次脱炭精錬炉の処理時間の延長や耐火
物コストの上昇、エネルギー使用量の増加等の問題が発
生している。
2. Description of the Related Art Conventionally, molten chromium-containing steel is decarburized to a carbon concentration of 0.3 to 1.0% by mass using a converter-type decarburizing and refining furnace such as a top-bottom blowing converter and a top-blowing converter. After melting the above-mentioned crude molten steel, the crude molten steel is tapped in a ladle. Then, in the decompression secondary decarburization refining process using this ladle, after adding an Al alloy for heating, the mixture is blown with acid to raise the temperature of the crude molten steel and perform the secondary decarburization refining, and then the chromium-containing molten steel. Is melted. Furthermore, in recent years,
In order to improve the workability of chromium-containing molten steel, the number of steel types aiming at low nitrogen (low N) is increasing, and although low N is being performed in the converter, it is not sufficient, and the decompression secondary decarburization refining treatment is not sufficient. Degassing is forced to be performed during the process of blowing acid decarburization refining, which causes problems such as extended processing time of the decompression secondary decarburization furnace, increased refractory costs, and increased energy consumption. Is occurring.

【0003】この対策として、特開昭58−18931
5号公報に記載されているように、転炉の出鋼口に出鋼
孔開閉装置を設け、この出鋼孔開閉装置に連通管を取り
付け、この連通管の先端を取鍋の内部に挿入し、更に、
蓋を用いて取鍋表面を覆ってアルゴンガスを内部に吹き
込んで低N及び低水素(H)溶鋼を溶製することが提案
されている。更に、特開昭58−189315号公報に
記載されているように、蓋を取り付けた取鍋内の溶鋼に
Ca合金を添加する際、Ca合金の強反応からボイルが
発生し、空気と溶鋼が接触して空気中の窒素の吸窒する
のを抑制するため、取鍋内のスラグに炭酸カルシウムや
苦灰石等のCO2 含有物質を添加し、取鍋内及びスラグ
内部をCO2 雰囲気にし、取鍋内の溶鋼が吸窒するのを
防止することが行われている。
As a countermeasure against this, Japanese Patent Laid-Open No. 58-18931
As described in Japanese Patent Publication No. 5, a tap hole opening / closing device is provided at the tap hole of the converter, a communicating pipe is attached to the tap hole opening / closing device, and the tip of the communicating pipe is inserted into the ladle. In addition,
It has been proposed to cover the surface of the ladle with a lid and blow argon gas into the interior to produce low N and low hydrogen (H) molten steel. Further, as described in JP-A-58-189315, when Ca alloy is added to molten steel in a ladle equipped with a lid, boil is generated due to strong reaction of Ca alloy and air and molten steel are separated from each other. In order to prevent the nitrogen in the air from coming into contact with the slag, a CO 2 -containing substance such as calcium carbonate or dolomite is added to the slag inside the ladle to create a CO 2 atmosphere inside the ladle and inside the slag. , It is carried out to prevent the molten steel in the ladle from being absorbed.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、特開昭
58−189315号公報に記載された方法では、転炉
の出鋼口に出鋼孔開閉装置や連通管、鍋蓋等の装置を要
し、設備が大がかりになり、設備費用の増加、あるいは
出鋼作業を外から監視することが困難になり、出鋼終了
の確認が容易でない。その結果、取鍋内に流入する転炉
スラグを抑制できない場合があり、減圧二次脱炭精錬時
に流入した転炉スラグに起因したクロム損失やスラグ過
剰に伴うオーバーフローや突沸等の事態を招き、操業が
不安定になる。更に、特開昭58−189315号公報
に記載された方法では、取鍋精錬での溶鋼の吸窒を抑制
できるが、含クロム溶鋼の転炉の還元処理過程における
吸窒や出鋼時の吸窒を防止することができない。
However, the method described in Japanese Patent Laid-Open No. 58-189315 requires a tap hole opening / closing device, a communicating pipe, a pot lid, and other devices at the tap hole of the converter. However, the equipment becomes large-scale, the equipment cost increases, or it becomes difficult to monitor the tapping operation from the outside, and it is not easy to confirm the tapping completion. As a result, it may not be possible to suppress the converter slag that flows into the ladle, causing a situation such as chromium loss due to the converter slag that has flowed in during the depressurization secondary decarburization and slag excess overflow or bumping, The operation becomes unstable. Further, in the method described in Japanese Patent Laid-Open No. 58-189315, it is possible to suppress the absorption of molten steel in ladle refining, but the absorption of nitrogen-containing molten steel in the reducing treatment process of the converter or during tapping. You cannot prevent nitriding.

【0005】その結果、減圧二次脱炭精錬時に脱窒する
ための脱ガス処理を行う必要が生じる。しかも、転炉で
の還元処理や出鋼中の吸窒を抑制できないと製品の窒素
(N)が高くなり、加工性等に優れた高純度溶鋼を溶製
することが出来ない。このように、特開昭58−189
315号公報に記載された方法の如く、取鍋精錬工程で
の吸窒を抑制しても、低窒素の高純度溶鋼を溶製するに
は、減圧二次脱炭精錬時に脱窒するための脱ガス処理は
回避できず、減圧二次脱炭精錬炉の処理時間の延長や耐
火物コストの上昇、エネルギー使用量の増加等の問題が
発生するという問題がある。
As a result, it is necessary to perform degassing treatment for denitrification during the depressurization secondary decarburization refining. In addition, if the reduction treatment in the converter and the absorption of nitrogen during tapping cannot be suppressed, the nitrogen (N) of the product becomes high, and it is impossible to produce high-purity molten steel excellent in workability and the like. As described above, Japanese Patent Laid-Open No. 58-189
As in the method described in Japanese Patent No. 315 gazette, even if nitrogen absorption in the ladle refining process is suppressed, in order to produce low-purity high-purity molten steel, denitrification is performed during depressurization secondary decarburization refining. The degassing process cannot be avoided, and there are problems that the processing time of the depressurized secondary decarburization and refining furnace is increased, the refractory cost is increased, and the energy consumption is increased.

【0006】本発明はかかる事情に鑑みてなされたもの
で、減圧二次脱炭精錬工程での脱ガス処理を軽減して低
窒素の高純度の含クロム溶鋼を溶製し、減圧二次脱炭精
錬炉の処理時間の短縮や耐火物コストの低減等を図るこ
とができる低窒素含クロム溶鋼の製造方法を提供するこ
とを目的とする。
The present invention has been made in view of the above circumstances. The degassing process in the depressurization secondary decarburizing and refining process is reduced to produce a high-purity chromium-containing molten steel with low nitrogen, and the secondary degassing under reduced pressure is performed. An object of the present invention is to provide a method for producing a low nitrogen chromium-containing molten steel capable of shortening the processing time of a coal refining furnace and reducing the cost of refractory materials.

【0007】[0007]

【課題を解決するための手段】前記目的に沿う本発明に
係る低窒素含クロム溶鋼の製造方法は、転炉内の脱炭精
錬を行った含クロム溶鋼に還元剤を添加した後にCO2
発生物質を分割添加し、スラグ中のクロム酸化物の還元
処理を行い、次いで、CO2 発生物質を入れた取鍋内に
前記還元処理を行った含クロム溶鋼を出鋼してから減圧
二次脱炭精錬を行う。この方法により、転炉での脱炭精
錬を行い炭素濃度が0.3〜1.0質量%に到達した時
点で、還元剤を添加するので、還元剤によるクロム酸化
物を含有した脱炭スラグの還元反応を促進し、同時に、
CO2 発生物質を分割して添加することにより、分解し
たCO2 ガスによって露出した粗溶鋼の表面を還元処理
期間中覆い、粗溶鋼の吸窒を抑制することができる。
The method for producing a low-nitrogen chromium-containing molten steel according to the present invention in accordance with the above-mentioned object is to reduce CO 2 after adding a reducing agent to the chromium-containing molten steel which has been decarburized and refined in a converter.
The generated substance is dividedly added to reduce the chromium oxide in the slag, and then the reduced chromium-containing molten steel is tapped into a ladle containing the CO 2 generating substance, and the secondary pressure reduction is performed. Perform decarburization refining. By this method, decarburization refining in the converter is performed, and when the carbon concentration reaches 0.3 to 1.0% by mass, the reducing agent is added. Therefore, the decarburizing slag containing chromium oxide by the reducing agent is added. Promotes the reduction reaction of
By dividing and adding the CO 2 -generating substance, the surface of the crude molten steel exposed by the decomposed CO 2 gas can be covered during the reduction treatment period, and the nitrogen absorption of the crude molten steel can be suppressed.

【0008】このCO2 発生物質にもよるが、例えば、
CO2 発生物質に炭酸カルシウムを用い、一括添加した
場合は、CO2 発生物質の吸熱により、スラグの流動性
が悪くなってクロム酸化物の還元速度が遅くなると共
に、その後の含クロム溶鋼の表面をCO2 ガスによる被
覆性も悪くなり、含クロム溶鋼の吸窒が激しくなる。こ
れに対し、CO2 発生物質を2分割以上にして添加する
と、急激なCO2 発生物質の吸熱を抑制し、極端なスラ
グの流動性の低下を招くことなく、クロム酸化物の還元
速度が良好な状態にでき、しかも、含クロム溶鋼の表面
は、CO2 ガスで継続的に覆われて含クロム溶鋼の吸窒
を抑制することができる。
Depending on the CO 2 generating substance, for example,
When calcium carbonate is used as the CO 2 generating substance and added all at once, the endothermic heat of the CO 2 generating substance deteriorates the fluidity of the slag and slows down the reduction rate of chromium oxide, and the surface of the molten chromium-containing steel thereafter. Of CO 2 gas also deteriorates the coverage of the molten chromium-containing steel, resulting in severe absorption of nitrogen. On the other hand, when the CO 2 -generating substance is added in two or more parts, the rapid endothermic absorption of the CO 2 -generating substance is suppressed and the reduction rate of chromium oxide is excellent without causing an extreme decrease in the fluidity of the slag. In addition, the surface of the molten chromium-containing steel can be continuously covered with CO 2 gas to suppress nitrogen absorption of the molten chromium-containing steel.

【0009】更に、出鋼時(炉傾転時)では、炉内をC
2 ガスの雰囲気にすることができないため、炉内に侵
入する空気からの含クロム溶鋼の吸窒を防ぐには、炉内
のスラグを溶融状態にして含クロム溶鋼を溶融したスラ
グで覆う必要があり、この条件を安定して満たすために
スラグの塩基度(CaO/SiO2 )を1.2〜1.7
好ましくは1.3〜1.4にすると良い。また、出鋼時
及び出鋼中の取鍋内の雰囲気をCO2 ガス雰囲気にして
いるので、粗溶鋼が空気と接触するのを抑制でき、低窒
素(N)の粗溶鋼を溶製することができる。
Furthermore, at the time of tapping (when the furnace is tilted), the inside of the furnace is C
Since it is not possible to create an atmosphere of O 2 gas, it is necessary to make the slag in the furnace in a molten state and cover the molten chromium-containing steel with molten slag in order to prevent nitrification of the molten chromium-containing steel from the air entering the furnace. In order to stably satisfy this condition, the basicity (CaO / SiO 2 ) of the slag is 1.2 to 1.7.
It is preferable to set it to 1.3 to 1.4. Further, since the atmosphere in the ladle during tapping and during tapping is a CO 2 gas atmosphere, it is possible to suppress the contact of the crude molten steel with air, and to produce the low nitrogen (N) crude molten steel. You can

【0010】本発明に係る低窒素含クロム溶鋼の製造方
法において、前記CO2 発生物質を入れた取鍋内の前記
含クロム溶鋼にスラグ低融点化剤を添加する。これによ
り、CO2 発生物質から生成したCO2 ガスによって含
クロム溶鋼が空気と接触するのを抑制すると共に、スラ
グ低融点化剤により取鍋内の含クロム溶鋼を溶融スラグ
で覆い、含クロム溶鋼の表面からの吸窒を抑制すること
ができる。
In the method for producing a low-nitrogen chromium-containing molten steel according to the present invention, a slag melting point reducing agent is added to the chromium-containing molten steel in the ladle containing the CO 2 generating substance. As a result, while preventing the molten chromium-containing steel from contacting the air with the CO 2 gas generated from the CO 2 -generating substance, the molten chromium-containing steel in the ladle is covered with the molten slag by the slag lowering agent, and the molten chromium-containing steel is obtained. It is possible to suppress nitrogen absorption from the surface.

【0011】本発明に係る低窒素含クロム溶鋼の製造方
法において、前記CO2 発生物質を炭酸カルシウムと
し、前記スラグ低融点化剤をSiO2 ・Al2 3 系か
らなるフラックスを用い、生成したCaO濃度に対する
SiO2 とAl2 3 濃度の比が1.3〜1.8になる
ように調整すると良い。これにより、取鍋内の含クロム
溶鋼を上に形成されるスラグを安定して溶融することが
可能になり、この溶融スラグで十分に覆うことができ
る。そして、含クロム溶鋼の表面からの吸窒を安定して
抑制するこができる。なお、生成したCaO濃度に対す
るSiO2 とAl23 濃度の比(CaO/SiO2
Al2 3 )が1.3未満、あるいは1.8を超える
と、スラグの流動性が低下し、出鋼から二次減圧脱炭精
錬における含クロム溶鋼の吸窒の防止効果が悪くなる。
In the method for producing a low nitrogen chromium-containing molten steel according to the present invention, the CO 2 generating substance is calcium carbonate, and the slag lowering agent is produced by using a flux of SiO 2 .Al 2 O 3 system. It is advisable to adjust the ratio of the SiO 2 and Al 2 O 3 concentrations to the CaO concentration to be 1.3 to 1.8. As a result, the slag formed on the molten steel containing chromium in the ladle can be stably melted, and the molten slag can be sufficiently covered. Further, it is possible to stably suppress nitrogen absorption from the surface of the chromium-containing molten steel. The ratio of the concentration of SiO 2 and Al 2 O 3 to the concentration of CaO generated (CaO / SiO 2 +
When Al 2 O 3 ) is less than 1.3 or exceeds 1.8, the fluidity of the slag is lowered, and the effect of preventing nitrogen absorption of the molten chromium-containing steel in the secondary decarburization refining from tapping is deteriorated.

【0012】本発明に係る低窒素含クロム溶鋼の製造方
法において、前記減圧二次脱炭精錬で前記含クロム溶鋼
に昇熱用Al合金を添加する。これにより、粗溶鋼の昇
熱を迅速に行うことができ、減圧二次脱炭精錬でのクロ
ムの酸化を抑制することができる。更に、本発明に係る
低窒素含クロム溶鋼の製造方法において、前記CO2
生物質が炭酸カルシウムであり、前記減圧二次脱炭精錬
で添加した昇熱用Al合金とが反応して生成したCaO
とAl2 3 の比が1.2〜1.6となるように調整す
ると良い。これにより、昇熱に使用して生成するAl2
3 をCO2 を発生した残りのCaOによって、減圧二
次脱炭スラグの流動性を向上し、含クロム溶鋼中に混在
するAl2 3 系の介在物を抑制することができる。
In the method for producing a low nitrogen chromium-containing molten steel according to the present invention, an Al alloy for heating is added to the chromium-containing molten steel in the reduced pressure secondary decarburization refining. This makes it possible to quickly raise the temperature of the crude molten steel and suppress the oxidation of chromium in the reduced pressure secondary decarburization refining. Further, in the method for producing a low nitrogen chromium-containing molten steel according to the present invention, the CO 2 generating substance is calcium carbonate, and CaO produced by reacting with the Al alloy for heat raising added in the reduced pressure secondary decarburization refining
It is advisable to adjust the ratio of Al 2 O 3 to 1.2 to 1.6. As a result, Al 2 generated by using for heating
The remaining CaO that has generated CO 2 from O 3 can improve the fluidity of the depressurized secondary decarburizing slag and can suppress Al 2 O 3 -based inclusions mixed in the molten chromium-containing steel.

【0013】CaOとAl2 3 の比(CaO/Al2
3 )が1.2未満になると、減圧二次脱炭スラグの流
動性が良くなり過ぎて取鍋の耐火物の損耗が増加し、溶
鋼中に混在するAl2 3 系の介在物も多くなり、含ク
ロム溶鋼の品質が低下する。一方、CaOとAl2 3
の比が1.6を超えると、減圧二次脱炭スラグの流動性
が悪くなり、生成した二次脱炭スラグ中のクロム酸化物
の還元処理に時間を要し、還元剤の使用量の増加を招
く。また、本発明に係る低窒素含クロム溶鋼の製造方法
において、前記取鍋の底部に設けたポーラスプラグの外
周囲をアルゴンガス雰囲気にシールすることが好まし
い。これにより、減圧二次脱炭精錬で取鍋内を攪拌する
ために必要なポーラスプラグの目地部から溶鋼中に侵入
する空気を遮断することができ、溶鋼の吸窒を防止する
ことができる。
The ratio of CaO to Al 2 O 3 (CaO / Al 2
When O 3 ) is less than 1.2, the fluidity of the depressurized secondary decarburization slag becomes too good, and the wear of the refractory in the ladle increases, and the inclusion of Al 2 O 3 -based inclusions in the molten steel also increases. However, the quality of molten steel containing chromium deteriorates. On the other hand, CaO and Al 2 O 3
If the ratio exceeds 1.6, the fluidity of the depressurized secondary decarburizing slag becomes poor, and it takes time to reduce the chromium oxide in the generated secondary decarburizing slag. Cause an increase. In addition, in the method for producing a low nitrogen chromium-containing molten steel according to the present invention, it is preferable to seal the outer periphery of the porous plug provided at the bottom of the ladle with an argon gas atmosphere. As a result, the air that enters the molten steel through the joints of the porous plug, which is necessary for stirring the inside of the ladle in the secondary decarburization under reduced pressure, can be blocked, and the absorption of nitrogen in the molten steel can be prevented.

【0014】[0014]

【発明の実施の形態】続いて、添付した図面を参照しつ
つ、本発明を具体化した実施の形態につき説明し、本発
明の理解に供する。図1は本発明の一実施の形態に係る
低窒素含クロム溶鋼の製造方法に適用される上底吹き転
炉の説明図、図2は同上底吹き転炉の出鋼の説明図、図
3は取鍋の底部に設けたポーラスプラグのシール構成の
説明図、図4は全CaO量と取鍋N値の関係を表すグラ
フ、図5は二次ブロー発生頻度を表すグラフである。
BEST MODE FOR CARRYING OUT THE INVENTION Next, referring to the attached drawings, an embodiment in which the present invention is embodied will be described to provide an understanding of the present invention. FIG. 1 is an explanatory view of an upper-bottom blowing converter applied to a method for producing a low-nitrogen chromium-containing molten steel according to an embodiment of the present invention, and FIG. 2 is an explanatory view of tapping of the upper-bottom blowing converter. Is an explanatory view of a sealing structure of a porous plug provided at the bottom of the ladle, FIG. 4 is a graph showing the relationship between the total CaO amount and the N value of the ladle, and FIG. 5 is a graph showing the secondary blow occurrence frequency.

【0015】図1〜図2に示すように、本発明の一実施
の形態に係る低窒素含クロム溶鋼の製造方法に用いられ
る転炉の一例である上底吹き転炉1は、炉体2の底部に
攪拌あるいは攪拌と燃料を兼ねた気体を吹き込むための
底吹きノズル3と、炉体2の上方側部に出鋼口4と、溶
銑や屑鉄、合金鉄(Fe−Cr)、生石灰、炭酸カルシ
ウム等の原料を装入する装入口5を設けている。更に、
装入口5の上方には、昇降自在に保持され、酸素を吹き
付けるランス6と、生石灰や還元剤等を炉体2内に投入
する副材ホッパ7を備えている。また、上底吹き転炉1
の炉体2を傾動して出鋼口4から粗溶鋼8を受ける底部
に攪拌用のアルゴンガスを供給するポーラスプラグ11
を取り付けた取鍋12と、この取鍋12の上方にCO2
ガス発生物質の一例である炭酸カルシウム13の貯蔵ホ
ッパ14を備えている。
As shown in FIGS. 1 and 2, an upper-bottom blown converter 1 which is an example of a converter used in a method for producing a low nitrogen chromium-containing molten steel according to an embodiment of the present invention comprises a furnace body 2 Bottom blowing nozzle 3 for blowing agitation or a gas that also serves as agitation and fuel to the bottom of the furnace, a tapping port 4 on the upper side of the furnace body 2, hot metal, scrap iron, ferroalloy (Fe-Cr), quick lime, A charging port 5 for charging a raw material such as calcium carbonate is provided. Furthermore,
Above the charging port 5, a lance 6 which is held so as to be vertically movable and blows oxygen, and an auxiliary material hopper 7 for feeding quicklime, a reducing agent, and the like into the furnace body 2 are provided. Also, the upper and lower blowing converter 1
Porous plug 11 for inclining the furnace body 2 and supplying argon gas for stirring to the bottom portion for receiving the crude molten steel 8 from the tapping port 4
CO 2 attached to the ladle 12 and above the ladle 12
A storage hopper 14 for storing calcium carbonate 13, which is an example of a gas generating substance, is provided.

【0016】図3は、取鍋の底部に設けたポーラスプラ
グのシール構成の説明図である。図3(a)は全体説明
であり、図3(b)はポーラスプラグ部の拡大図であ
る。この図3(a)および図3(b)に示すように、取
鍋12の底部に取り付けたポーラスプラグ11は、取鍋
鉄皮20に穿ったポーラスプラグ11の挿入孔から内張
り耐火物15に目地16を介して装着される。ポーラス
プラグ11の下方は、円板状のシール鉄板17aとシー
ル鉄板17bの間に複数の孔18を穿った内部を中空に
したリング19を設けており、特に、シール鉄板17b
は取鍋鉄皮20に面接触してリークがないようにしてい
る。アルゴンガスは、ポーラスプラグ11には、アルゴ
ンガス管21から供給され、リング19には、シールガ
ス管22から供給される。なお、符号9は脱炭精錬を終
了した時点の転炉スラグ、符号10は還元処理を終了
し、炭酸カルシウムを添加した後のスラグである。
FIG. 3 is an explanatory view of the sealing structure of the porous plug provided at the bottom of the ladle. FIG. 3A is a general description, and FIG. 3B is an enlarged view of the porous plug portion. As shown in FIGS. 3 (a) and 3 (b), the porous plug 11 attached to the bottom portion of the ladle 12 is provided with a lining refractory material 15 through an insertion hole of the porous plug 11 formed in the ladle iron shell 20. It is attached through the joint 16. Below the porous plug 11, there is provided a ring 19 having a hollow interior with a plurality of holes 18 formed between a disk-shaped seal iron plate 17a and a seal iron plate 17b.
Is in contact with the ladle iron skin 20 so that there is no leak. The argon gas is supplied to the porous plug 11 from an argon gas pipe 21, and the ring 19 is supplied from a seal gas pipe 22. Reference numeral 9 is a converter slag when the decarburization refining is completed, and reference numeral 10 is a slag after the reduction treatment is completed and calcium carbonate is added.

【0017】次に、上底吹き転炉1を用い本実施の形態
に係る低窒素含クロム溶鋼の製造方法について説明す
る。上底吹き転炉1の炉体2内に装入口5から溶銑と屑
鉄、生石灰等を装入し、底吹きノズル3から攪拌用のガ
スを吹き込みながらランス6を下降して酸素を吹き付け
る吹酸を開始した。炉体2内の温度が1500℃以上に
なってからFe−Cr合金を添加し、引き続きランス6
からの吹酸と底吹きノズル3からの拌用ガスの吹き込み
により、脱炭精錬を行った。そして、炭素濃度が0.3
〜1.0質量%となった時点で、吹酸を停止し、ランス
6を上昇して脱炭精錬を終了した。この時の転炉スラグ
9は、クロム酸化物(Cr2 3 )を多量に含むため、
流動性が悪く、粗溶鋼8の表面を十分に覆う状態にな
く、吹酸の終了と同時に炉体2内に空気が侵入し、底吹
きノズル3から攪拌用のガスによって粗溶鋼8の表面が
露出して空気と接触する状態にある。
Next, a method for manufacturing the low nitrogen chromium-containing molten steel according to the present embodiment using the upper-bottom blowing converter 1 will be described. Blast acid for charging hot metal, scrap iron, quicklime, etc. into the furnace body 2 of the top-bottom blowing converter 1 from the charging port 5 and lowering the lance 6 while blowing a gas for stirring from the bottom-blowing nozzle 3 to blow oxygen Started. After the temperature inside the furnace body 2 reached 1500 ° C or higher, the Fe-Cr alloy was added, and then the lance 6 was added.
The decarburization refining was performed by blowing in the blowing acid from No. 3 and the stirring gas from the bottom blowing nozzle 3. And the carbon concentration is 0.3
At the time when the content reached ˜1.0% by mass, the blowing acid was stopped and the lance 6 was raised to complete the decarburization refining. Since the converter slag 9 at this time contains a large amount of chromium oxide (Cr 2 O 3 ),
Since the fluidity is poor and the surface of the crude molten steel 8 is not sufficiently covered, air enters the furnace body 2 at the same time as the end of the blowing acid, and the surface of the crude molten steel 8 is agitated by the gas for stirring from the bottom blowing nozzle 3. Exposed and in contact with air.

【0018】従って、転炉スラグ9に還元剤の一例であ
るFe−Si合金を添加し、Fe−Si合金の分散と溶
解を完了し、すなわちFe−Si合金を添加してから
0.3〜1.5分後に速やかに炭酸カルシウム(CaC
3 )を副材ホッパから切り出し0.5〜1.0トン/
チャージ添加する。このCaCO3 の添加により、熱分
解したCO2 ガスが炉体2内に充満し、炉内への空気の
侵入を抑制すると共に、粗溶鋼8の表面が空気と接触す
るのを防止する。しかし、第1回目のCaCO3添加か
ら1.6〜3.0分以内に第2回目のCaCO3 添加を
0.5〜1.0トン/チャージ添加する。この分割添加
により、炉体2内をCO2 ガスで置換し、多量にCr2
3 を含み流動性の悪い十分なスラグカバー効果の発現
できない還元処理の初期から中期における粗溶鋼8の表
面が空気と接触するのを確実に抑制して粗溶鋼8の窒素
の吸窒を防止することができる。
Therefore, the Fe-Si alloy, which is an example of a reducing agent, is added to the converter slag 9 to complete the dispersion and dissolution of the Fe-Si alloy, that is, 0.3 to 0.3% after the addition of the Fe-Si alloy. Promptly after 1.5 minutes calcium carbonate (CaC
Cut out the O 3) from Fukuzai hopper 0.5 to 1.0 t /
Add charge. The addition of CaCO 3 fills the furnace body 2 with the thermally decomposed CO 2 gas, suppresses the intrusion of air into the furnace, and prevents the surface of the crude molten steel 8 from coming into contact with air. However, within the range of 1.6 to 3.0 minutes from the first addition of CaCO 3 , the second addition of CaCO 3 is added at 0.5 to 1.0 ton / charge. By this divided addition, the inside of the furnace body 2 is replaced with CO 2 gas, and a large amount of Cr 2 is added.
Prevents nitrogen absorption of crude molten steel 8 by reliably suppressing contact of the surface of crude molten steel 8 with air in the early to middle stages of the reduction treatment that contains O 3 and cannot express a sufficient slag cover effect with poor fluidity. can do.

【0019】更に、前記したCaCO3 の添加を分割添
加にして転炉スラグ9が急激な吸熱によって流動性が低
下するのを抑制することができ、しかも、転炉スラグ9
の塩基度を1.2〜1.7、好ましくは1.3〜1.4
になるように調整しているので、転炉スラグ9を溶融状
態で流動性をより良好にすることができ、よりスラグカ
バー効果を十分に発現することができる。このようにし
て、還元処理を4〜6分間行った後、炉体2を傾動して
出鋼口4から粗溶鋼8を取鍋12に出鋼する。この取鍋
12への粗溶鋼8の出鋼時に、貯蔵ホッパ14から取鍋
12内に炭酸カルシウム(CaCO3 )を0.1〜0.
5トン/鍋と、スラグ低融点化剤の一例であるSiO2
・Al2 3 系からなる例えばSiO2 が38質量%、
Al2 3 が25質量%、残部がCaOの組成からなる
ものを100〜150kg/鍋入れ置きしておく。更
に、取鍋12の底部に設けたポーラスプラグ11に、ア
ルゴンガス管21から供給されたアルゴンガスの吹き込
みを受湯の直後から行う。
Further, the above-mentioned CaCO3The addition of
In addition, the converter slag 9 has low fluidity due to the rapid heat absorption.
It is possible to suppress lowering, and moreover, converter slag 9
Has a basicity of 1.2 to 1.7, preferably 1.3 to 1.4
Is adjusted so that the converter slag 9 is melted.
Can improve the fluidity in the
The bar effect can be sufficiently expressed. Like this
Then, after performing the reduction treatment for 4 to 6 minutes, the furnace body 2 is tilted.
The crude molten steel 8 is tapped into the ladle 12 from the tapping port 4. This ladle
Ladle from the storage hopper 14 at the time of tapping the crude molten steel 8 to the 12
Calcium carbonate (CaCO3) From 0.1 to 0.
5 ton / pot and SiO which is an example of a slag melting point reducing agent2
・ Al2O3Made of a system such as SiO2Is 38% by mass,
Al2O 3Is composed of 25 mass% and the balance is CaO.
Put 100-150 kg / pot in a pot. Change
The porous plug 11 on the bottom of the ladle 12
Blow-in of argon gas supplied from Lugon gas pipe 21
Do the hot water immediately after receiving the hot water.

【0020】取鍋12内に入れ置きしたCaCO3 は、
粗溶鋼8の熱により、CaOとCO 2 に分解反応を起こ
し、発生したCO2 が取鍋12内をCO2 雰囲気にして
空気の侵入を防止することができ、粗溶鋼8の低窒素化
を図ることができる。しかも、添加したCaCO3 が分
解した後のCaOがスラグ低融点化剤と反応して速やか
に溶融したスラグを生成することができる。また、この
CaCO3 が分解した後のCaO濃度に対するSiO2
+Al2 3 濃度の比〔CaO/(SiO2 +Al2
3 )〕が1.3〜1.8となるように、スラグ低融点化
剤の添加量を調整するか、あるいはCaO、又はSiO
2 やAl2 3 を添加して前記した濃度の比を満たすよ
うに調整することができる。
CaCO placed in the ladle 123Is
Due to the heat of the crude molten steel 8, CaO and CO 2Cause a decomposition reaction
CO generated2CO in the ladle 122In the atmosphere
It is possible to prevent air from entering and reduce the nitrogen content of the crude molten steel 8.
Can be achieved. Moreover, the added CaCO3Minutes
CaO after unraveling reacts quickly with the slag lowering agent
The molten slag can be generated. Also this
CaCO3Of CaO concentration after decomposition of SiO2
+ Al2O3Concentration ratio [CaO / (SiO2+ Al2O
3)] Is 1.3 to 1.8 so that the melting point of the slag is lowered.
Adjusting the amount of agent added, or CaO or SiO
2And Al2O3To meet the above concentration ratio
Can be adjusted.

【0021】そして、粗溶鋼8の表面を覆う十分なカバ
ースラグを形成することができるため、粗溶鋼8の表面
が直接に空気と接触するのを回避し、しかも、取鍋12
を炉体2の下部から減圧二次脱炭精錬装置(図示せず)
まで輸送する過程で、ポーラスプラグ11から吹き込ま
れたアルゴンガスのボイル等に起因する粗溶鋼8と空気
の接触するのを防止することができる。更に、取鍋12
の底部に設けたポーラスプラグ11の取鍋鉄皮20に穿
った挿入孔から内張り耐火物15に目地16を介して装
着されたポーラスプラグ11の下方には、円板状のシー
ル鉄板17aとシール鉄板17bの間に複数の孔18を
穿った中空のリング19に、シールガス管22からアル
ゴンガスを供給し、中空のリング19の複数の孔18か
ら吹き出したアルゴンガスにより、ポーラスプラグ18
と内張り耐火物15の目地16との隙間から侵入する外
気(空気)を遮断するようにしている。
Since sufficient cover slag for covering the surface of the crude molten steel 8 can be formed, direct contact of the surface of the crude molten steel 8 with air can be avoided, and the ladle 12 can be used.
From the lower part of the furnace body 2 to a decompression secondary decarburization refining device (not shown)
It is possible to prevent air from coming into contact with the crude molten steel 8 due to boil of argon gas blown from the porous plug 11 in the process of transporting to. Furthermore, ladle 12
At the bottom of the porous plug 11 attached to the lining refractory 15 through the joint 16 from the insertion hole formed in the ladle iron skin 20 of the porous plug 11 provided at the bottom of the disk, a disk-shaped seal iron plate 17a and a seal are provided. Argon gas is supplied from a seal gas pipe 22 to a hollow ring 19 having a plurality of holes 18 between the iron plates 17b, and the porous plug 18 is supplied by the argon gas blown from the plurality of holes 18 of the hollow ring 19.
The outside air (air) entering through the gap between the joint 16 of the refractory lining 15 and the joint 16 is blocked.

【0022】更に、炉体2から出鋼された粗溶鋼8は、
温度を補償するため、昇熱剤の一例である金属Alを添
加して昇熱した後、減圧二次脱炭精錬が行われる。しか
し、金属Alが燃焼して生成したスラグ中のAl2 3
の濃度が高くなると製品となる含クロム溶鋼中にAl2
3 系の介在物が増加し、鋳片や鋼材の品質を阻害する
ことになる。そこで、取鍋12に入れ置きし、分解して
生成したCaOを有効活用して、減圧二次脱炭精錬にお
いて添加した金属Alが燃焼して生成したAl 2 3
濃度の値をCaO/Al2 3 が1.2〜1.6となる
ように金属Alや生石灰等の添加を考慮して調整する。
Further, the crude molten steel 8 tapped from the furnace body 2 is
In order to compensate for the temperature, metal Al, which is an example of a heating agent, is added.
After adding and heating, decompression secondary decarburization refining is performed. Only
Al in the slag generated by the combustion of metallic Al2O3
When the concentration of Al increases, Al becomes2
O3Inclusions in the system increase and impair the quality of cast and steel products
It will be. So, put it in the ladle 12 and disassemble it.
Effectively utilizing the generated CaO for decompression secondary decarburization refining
Al produced by combustion of added metallic Al 2O3of
Concentration value is CaO / Al2O3Becomes 1.2 to 1.6
As described above, adjustment is performed in consideration of addition of metallic Al, quick lime, and the like.

【0023】その結果、減圧二次脱炭スラグの流動性が
向上し、含クロム溶鋼中に混在するAl2 3 系の介在
物を抑制することができ、二次脱炭スラグ中のクロム酸
化物の還元処理を速やかに行うことができ、還元処理時
間の短縮や還元剤の使用の節減が可能になる。そして、
図4に示すように、還元処理時にCaCO3 を添加しな
い従来の含クロム粗溶鋼の窒素濃度が100〜200p
pmと高いのに対し、本実施の形態の場合では、窒素濃
度が40〜90ppmの極低窒素の含クロム粗溶鋼8を
溶製でき、減圧二次脱炭精錬装置を用いて二次脱炭精錬
を行うことにより、窒素濃度が40〜90ppmの極低
窒素の含クロム溶鋼を溶製することができた。この鋳片
を加工した鋼材の加工性等の品質を向上することができ
る。
As a result, the fluidity of the depressurized secondary decarburizing slag is improved, the Al 2 O 3 -based inclusions mixed in the molten chromium-containing steel can be suppressed, and the chromium oxidation in the secondary decarburizing slag is suppressed. The reduction treatment of the substance can be performed promptly, and the reduction treatment time and the use of the reducing agent can be reduced. And
As shown in FIG. 4, the nitrogen concentration of the conventional Cr-containing crude molten steel to which CaCO 3 is not added during the reduction treatment has a nitrogen concentration of 100 to 200 p.
In contrast to the high pm, in the case of the present embodiment, the extremely low nitrogen chromium-containing crude molten steel 8 having a nitrogen concentration of 40 to 90 ppm can be smelted, and the secondary decarburization is performed by using a reduced pressure secondary decarburization refining device. By performing refining, it was possible to produce an extremely low nitrogen chromium-containing molten steel having a nitrogen concentration of 40 to 90 ppm. It is possible to improve the workability and other qualities of the steel material processed from this slab.

【0024】[0024]

【実施例】次に、低窒素含クロム溶鋼の製造方法の実施
例について説明する。上底吹き転炉の炉内に装入口から
溶銑(30トン)の溶銑と、屑鉄を装入し、副材ホッパ
からFe・Cr合金、生石灰等副原料を装入し、炉体に
設けた底吹きノズルから攪拌用のガスを吹き込みながら
ランスを下降して酸素を28000Nm 3 /時間の吹酸
速度で吹酸を開始行い、炉内の温度が1500℃以上に
なってからFe−Cr合金を添加し、引き続きランスか
らの吹酸と底吹きノズルからの拌用ガスの吹き込みによ
り、炭素濃度が0.3〜1.0質量%になるまで脱炭精
錬を終了した。
[Examples] Next, implementation of a method for producing low nitrogen chromium-containing molten steel
An example will be described. From the charging port into the furnace of the top-bottom blow converter
Hot metal (30 tons) of hot metal and scrap iron are charged, and a hopper for auxiliary material
Fe / Cr alloy, quicklime and other auxiliary materials are charged into the furnace body
While blowing a stirring gas from the bottom blowing nozzle provided
Lower the lance and add oxygen to 28,000 Nm 3/ Hour of acid
Starts blowing acid at a high speed and raises the temperature in the furnace to 1500 ° C or higher.
After that, add Fe-Cr alloy and continue
And the blowing gas from the bottom blowing nozzle.
Decarburization until the carbon concentration reaches 0.3 to 1.0 mass%
Ren finished.

【0025】脱炭精錬を終了後、炉内にFe−Si合金
を添加し、0.3〜1.5分後に速やかに炭酸カルシウ
ム(CaCO3 )を副材ホッパから切り出し0.5〜
1.0トン/チャージ添加し、更に、第1回目のCaC
3 添加から1.6〜3.0分以内に第2回目のCaC
3 添加を0.5〜1.0トン/チャージ添加して転炉
のスラグの還元処理を行い転炉スラグ中のCr2 3
Crとして粗溶鋼中に回収した。還元処理を終了した粗
溶鋼を、貯蔵ホッパから取鍋内に炭酸カルシウム(Ca
CO3 )を0.1〜0.5トン/鍋と、SiO2 ・Al
2 3 系のスラグ低融点化剤100kgを入れ置きた取
鍋に出鋼した。この粗溶鋼をVOD等の減圧二次脱炭精
錬装置を用いて、金属Alの添加による昇熱と吹酸の脱
炭精錬を行った。更に、取鍋では、底部に設けたポーラ
スプラグからアルゴンガスを400〜600Nm3 /時
間吹き込みを連続鋳造するまで行った。
After the decarburization refining is completed, the Fe-Si alloy is added into the furnace, and after 0.3 to 1.5 minutes, calcium carbonate (CaCO 3 ) is cut out from the auxiliary material hopper and 0.5 to
Add 1.0 ton / charge, and then the first CaC
2nd CaC within 1.6-3.0 minutes after addition of O 3
O 3 was added in an amount of 0.5 to 1.0 ton / charge to reduce the slag in the converter, and Cr 2 O 3 in the converter slag was recovered as Cr in the crude molten steel. The crude molten steel that has undergone the reduction treatment is transferred from the storage hopper to a calcium carbonate (Ca
CO 3 ) 0.1 to 0.5 ton / pot and SiO 2 · Al
The steel was tapped into a ladle containing 100 kg of a 2 O 3 -based slag lowering agent. This crude molten steel was subjected to decarburization refining of fumaric acid by raising the temperature by adding metal Al using a decompression secondary decarburization refining device such as VOD. Further, in the ladle, argon gas was blown at 400 to 600 Nm 3 / hour from a porous plug provided at the bottom until continuous casting.

【0026】実施例1は、転炉での還元処理時に、Fe
−Si合金を添加してから1.0分を経過した後、炭酸
カルシウムを0.5トン/チャージ添加し、更に、第1
回目のCaCO3 添加から2.0分後に第2回目のCa
CO3 を0.5トン/チャージ添加して転炉のスラグの
還元処理を行い、取鍋に炭酸カルシウムを0.3トン/
鍋とスラグ低融点化剤100kgを入れ置し、その後減
圧二次脱炭精錬を行った場合であり、窒素濃度が60p
pmの含クロム溶鋼を溶製することができ、図5に示す
ように減圧二次脱炭精錬での二次ブロー(減圧脱炭精錬
の途中に脱ガス処理を行う場合)の発生頻度が0.09
と良好であった。
In Example 1, Fe reduction was performed during the reduction treatment in the converter.
1.0 minute after the addition of the Si alloy, 0.5 ton / charge of calcium carbonate was added, and
2.0 minutes after the second CaCO 3 addition, the second Ca
Add 0.5 ton of CO 3 / charge to reduce converter slag and add 0.3 ton of calcium carbonate to ladle
This is the case where a pot and 100 kg of the slag lowering agent are placed and then the secondary decarburization refining under reduced pressure is performed, and the nitrogen concentration is 60 p.
It is possible to produce pm chromium-containing molten steel, and as shown in FIG. 5, the occurrence frequency of secondary blow (when degassing treatment is performed during the reduced pressure decarburization refining) in the reduced pressure secondary decarburization refining is 0. .09
And was good.

【0027】実施例2は、転炉での還元処理時に、Fe
−Si合金を添加してから1.0分を経過した後、炭酸
カルシウムを0.5トン/チャージ添加し、更に、第1
回目のCaCO3 添加から2.0分後に第2回目のCa
CO3 を1.0トン/チャージ添加して転炉のスラグの
還元処理を行い、取鍋に炭酸カルシウムを0.3トン/
鍋とスラグ低融点化剤100kgを入れ置し、その後減
圧二次脱炭精錬を行い、取鍋の底部のポーラスプラグの
目地部からの空気の侵入をアルゴンガスでシールした場
合であり、窒素濃度が40ppmの含クロム溶鋼を溶製
することができ、図5に示すように減圧二次脱炭精錬で
の二次ブローの発生頻度が0.07と極めて良好であっ
た。
In Example 2, Fe during Fe reduction treatment was used.
1.0 minute after the addition of the Si alloy, 0.5 ton / charge of calcium carbonate was added, and
2.0 minutes after the second CaCO 3 addition, the second Ca
Add 1.0 ton of CO 3 / charge to reduce converter slag and add 0.3 ton of calcium carbonate to ladle
This is a case where a pot and 100 kg of a slag melting point reducing agent are placed, after which secondary vacuum decarburization and refining are performed, and the invasion of air from the joint part of the porous plug at the bottom of the ladle is sealed with argon gas, the nitrogen concentration It was possible to smelt a chromium-containing molten steel of 40 ppm, and as shown in FIG. 5, the occurrence frequency of secondary blow in the reduced pressure secondary decarburization refining was 0.07, which was extremely good.

【0028】実施例3は、転炉での還元処理時に、Fe
−Si合金を添加してから1.0分を経過した後、炭酸
カルシウムを0.5トン/チャージ添加し、更に、第1
回目のCaCO3 添加から2.0分後に第2回目のCa
CO3 を0.5トン/チャージ添加して転炉のスラグの
還元処理を行い、取鍋に炭酸カルシウムを0.3トン/
鍋とスラグ低融点化剤100kgを入れ置し、その後減
圧二次脱炭精錬のCaO/Al2 3 を1.2〜1.5
に調整した場合であり、窒素濃度が60ppmの含クロ
ム溶鋼を溶製することができ、しかも、含クロム溶鋼の
Al2 3 系介在物の欠陥を防止することができた。
In Example 3, during the reduction treatment in the converter, Fe
1.0 minute after the addition of the Si alloy, 0.5 ton / charge of calcium carbonate was added, and
2.0 minutes after the second CaCO 3 addition, the second Ca
Add 0.5 ton of CO 3 / charge to reduce converter slag and add 0.3 ton of calcium carbonate to ladle
A pot and 100 kg of the slag deliquescent agent are placed, and then CaO / Al 2 O 3 of the secondary decarburization under reduced pressure is added to 1.2 to 1.5.
It was possible to produce molten chromium-containing steel having a nitrogen concentration of 60 ppm, and it was possible to prevent defects of Al 2 O 3 -based inclusions in the molten chromium-containing steel.

【0029】これに対し、転炉での還元処理時にFe−
Si合金を添加し、この還元処理の途中に炭酸カルシウ
ムを添加せず、更に、取鍋にも炭酸カルシウムを入れ置
しなかった場合であり、図5に示すように二次ブローの
発生頻度が0.20と極めて悪く、窒素濃度が150p
pmと高くなった。以上、本発明の実施の形態を説明し
たが、本発明は、上記した形態に限定されるものでな
く、要旨を逸脱しない条件の変更等は全て本発明の適用
範囲である。例えば、CO2 発生物質としては、炭酸カ
ルシウムの他に、炭酸マグネシウム、や生ドロマイト等
の炭酸化合物を使用することができる。更に、転炉での
還元剤の添加後に、炭酸カルシウムを連続して投入する
こともでき、常に粗溶鋼の表面をCO2 で覆うので好ま
しい。
On the other hand, during the reduction treatment in the converter, Fe-
This is a case where Si alloy was added, calcium carbonate was not added during the reduction treatment, and calcium carbonate was not placed in the ladle. As shown in FIG. Extremely bad at 0.20, nitrogen concentration 150p
It was as high as pm. Although the embodiments of the present invention have been described above, the present invention is not limited to the above-described embodiments, and all modifications and the like of the conditions without departing from the gist are within the scope of the present invention. For example, as the CO 2 generating substance, in addition to calcium carbonate, magnesium carbonate or a carbonate compound such as raw dolomite can be used. Further, calcium carbonate can be continuously added after the reducing agent is added in the converter, and the surface of the crude molten steel is always covered with CO 2, which is preferable.

【0030】[0030]

【発明の効果】以上述べたように、本発明による、転炉
内の脱炭精錬を行った含クロム溶鋼に還元剤を添加した
後にCO2 発生物質を分割添加し、スラグ中のクロム酸
化物の還元処理を行い、次いで、CO2 発生物質を入れ
た取鍋内に還元処理を行った含クロム溶鋼を出鋼してか
ら減圧二次脱炭精錬を行うので、減圧二次脱炭精錬工程
での脱ガス処理を軽減して低窒素の高純度溶鋼を溶製
し、減圧二次脱炭精錬炉の処理時間の短縮や耐火物コス
トの低減等を図ることができる。
As described above, according to the present invention, the reducing agent is added to the decarburized and smelted chromium-containing steel in the converter, and then the CO 2 -generating substance is dividedly added to the chromium oxide in the slag. Is performed, and then the reduced-pressure secondary decarburization refining process is performed after tapping the reduced chromium-containing molten steel in the ladle containing the CO 2 -generating substance. It is possible to reduce the degassing treatment in step 1 to produce low-nitrogen high-purity molten steel, and shorten the processing time of the reduced pressure secondary decarburizing and refining furnace and the cost of refractory materials.

【0031】特に、請求項2記載の低窒素含クロム溶鋼
の製造方法は、CO2 発生物質を入れた取鍋内の含クロ
ム溶鋼にスラグ低融点化剤を添加するので、CO2 発生
物質から生成したCO2 ガスとスラグ低融点化剤により
溶融したスラグで、取鍋内の含クロム溶鋼の表面を覆う
ことの相乗効果により、含クロム溶鋼の表面からの吸窒
を抑制することができる。
[0031] In particular, the production method of low nitrogen containing chromium molten steel according to claim 2, since the addition of slag low melting agent to chromium-containing molten steel in the ladle containing the CO 2 generating material, the CO 2 generating material The synergistic effect of covering the surface of the molten chromium-containing steel in the ladle with the generated CO 2 gas and the slag melted by the slag melting point reducing agent can suppress the absorption of nitrogen from the surface of the molten chromium-containing steel.

【0032】また、請求項3記載の低窒素含クロム溶鋼
の製造方法は、CO2 発生物質を炭酸カルシウムとし、
前記スラグ低融点化剤をSiO2 ・Al2 3 系からな
るフラックスを用い、生成したCaO濃度に対するSi
2 とAl2 3 濃度の比が1.3〜1.8になるよう
に調整するので、取鍋内の含クロム溶鋼を上に形成され
るスラグを安定して溶融させ、溶融スラグで含クロム溶
鋼の表面を十分に覆うことができ、含クロム溶鋼の表面
からの吸窒を安定して抑制するこができる。
Further, in the method for producing a low nitrogen chromium-containing molten steel according to claim 3, the CO 2 generating substance is calcium carbonate,
As the slag lowering agent, a flux composed of a SiO 2 · Al 2 O 3 system is used, and Si for the generated CaO concentration is used.
Since the ratio of O 2 and Al 2 O 3 concentration is adjusted to 1.3 to 1.8, the slag formed on the molten chromium-containing steel in the ladle is stably melted, and the molten slag is used. The surface of the chromium-containing molten steel can be sufficiently covered and the nitrogen absorption from the surface of the chromium-containing molten steel can be stably suppressed.

【0033】また、請求項4記載の低窒素含クロム溶鋼
の製造方法は、減圧二次脱炭精錬で含クロム溶鋼に昇熱
用Al合金を添加するので、粗溶鋼の昇熱を迅速に行う
ことができ、減圧二次脱炭精錬でのクロムの酸化を抑制
することができ、還元剤をも節減することができる。ま
た、請求項5記載の低窒素含クロム溶鋼の製造方法は、
CO2 発生物質が炭酸カルシウムであり、減圧二次脱炭
精錬で添加した昇熱用Al合金とが反応して生成したC
aOとAl2 3 の比が1.2〜1.6となるように調
整するので、昇熱に使用して生成したAl2 3 による
スラグの高融点化を抑制して減圧二次脱炭スラグの流動
性を向上して脱炭反応と酸化クロムの還元を促進し、取
鍋の耐火物の損耗を抑制やAl2 3 系の介在物に起因
する鋳片及び鋼材の欠陥の発生を防止し、鋳片及び鋼材
の品質を向上することができる。
Further, in the method for producing a low nitrogen chromium-containing molten steel according to claim 4, since the Al alloy for heating is added to the chromium-containing molten steel in the reduced pressure secondary decarburization refining, the heating of the crude molten steel is rapidly carried out. It is possible to suppress the oxidation of chromium in the secondary decarburization and refining under reduced pressure, and to reduce the reducing agent. Further, the method for producing a low nitrogen chromium-containing molten steel according to claim 5,
The CO 2 generating substance is calcium carbonate, and C generated by reacting with the Al alloy for heat raising added in the secondary decarburization under reduced pressure
Since the ratio of aO to Al 2 O 3 is adjusted to 1.2 to 1.6, the high melting point of slag due to Al 2 O 3 used for heating is suppressed to suppress the secondary decompression of the slag. Improves the fluidity of the charcoal slag, promotes the decarburization reaction and the reduction of chromium oxide, suppresses the wear of the refractory of the ladle, and causes the defects of cast slabs and steels caused by Al 2 O 3 inclusions. Can be prevented and the quality of the cast slab and the steel material can be improved.

【0034】さらに、請求項6記載の低窒素含クロム溶
鋼の製造方法は、取鍋の底部に設けたポーラスプラグの
外周囲をアルゴンガス雰囲気にシールするので、転炉の
出鋼から減圧二次脱炭精錬中にポーラスプラグの目地部
から溶鋼中に侵入する空気からの溶鋼の吸窒を防止する
ことができ、極低窒素の含クロム溶鋼を製造することが
できる。
Further, according to the method for producing low-nitrogen chromium-containing molten steel according to claim 6, since the outer periphery of the porous plug provided at the bottom of the ladle is sealed with an argon gas atmosphere, a secondary pressure reduction from the steel output from the converter is performed. It is possible to prevent nitrification of molten steel from the air that enters the molten steel from the joints of the porous plug during decarburization refining, and it is possible to manufacture chromium-containing molten steel with extremely low nitrogen.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の一実施の形態に係る低窒素含クロム溶
鋼の製造方法に適用される上底吹き転炉の説明図であ
る。
FIG. 1 is an explanatory view of an upper-bottom blowing converter applied to a method for producing a low-nitrogen chromium-containing molten steel according to an embodiment of the present invention.

【図2】同上底吹き転炉の出鋼の説明図である。FIG. 2 is an explanatory view of a tapped steel of the upper bottom blowing converter.

【図3】取鍋の底部に設けたポーラスプラグのシール構
成の説明図である。
FIG. 3 is an explanatory diagram of a seal configuration of a porous plug provided at the bottom of a ladle.

【図4】全CaO量と取鍋N値の関係を表すグラフであ
る。
FIG. 4 is a graph showing the relationship between the total CaO amount and the ladle N value.

【図5】二次ブロー発生頻度を表すグラフである。FIG. 5 is a graph showing a secondary blow occurrence frequency.

【符号の説明】[Explanation of symbols]

1 上底吹き転炉 2 炉体 3 底吹きノズル 4 出鋼口 5 装入口 6 ランス 7 副材ホッパ 8 粗溶鋼 9 転炉スラグ 10 炭酸カルシウムを添加した後のスラグ 11 ポーラスプラグ 12 取鍋 13 炭酸カルシウム 14 貯蔵ホッパ 15 内張り耐火物 16 目地 17a、17b シール鉄板 18 孔 19 リング 20 取鍋鉄皮 21 アルゴンガス管 22 シールガス管 1 Top-bottom blowing converter 2 furnace body 3 bottom blowing nozzle 4 Steel tap 5 booth 6 Lance 7 Secondary material hopper 8 Crude molten steel 9 Converter slag 10 Slag after adding calcium carbonate 11 Porous plug 12 ladle 13 calcium carbonate 14 Storage hopper 15 Refractory lining 16 joints 17a, 17b Sealed iron plate 18 holes 19 ring 20 Ladle iron skin 21 Argon gas pipe 22 Seal gas pipe

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C21C 7/072 C21C 7/072 Z 7/076 7/076 A (72)発明者 今村 智之 福岡県北九州市戸畑区飛幡町1番1号 新 日本製鐵株式会社八幡製鐵所内 (72)発明者 高塚 昇 福岡県北九州市戸畑区飛幡町1番1号 新 日本製鐵株式会社八幡製鐵所内 (72)発明者 早川 隆造 福岡県北九州市戸畑区飛幡町1番1号 新 日本製鐵株式会社八幡製鐵所内 (72)発明者 渡邊 涼 福岡県北九州市戸畑区飛幡町1番1号 新 日本製鐵株式会社八幡製鐵所内 Fターム(参考) 4K013 AA02 BA02 BA12 CA02 CB09 CF13 DA03 DA08 DA10 DA12 EA01 EA12 EA19 4K070 AA03 AB03 AB07 AB17 AC20 AC23 BD09 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) C21C 7/072 C21C 7/072 Z 7/076 7/076 A (72) Inventor Tomoyuki Imamura Kitakyushu City, Fukuoka Prefecture No. 1-1 Tobata-cho, Tobata-ku, Yawata Works, New Steel Co., Ltd. (72) Inventor Noboru Takatsuka No. 1-1, Tobata-cho, Tobata-ku, Kitakyushu, Fukuoka Prefecture (72), Yawata Works, Nippon Steel Co., Ltd. (72) Inventor Ryuzo Hayakawa 1-1 Hibatacho, Tobata-ku, Kitakyushu, Fukuoka Prefecture Inside the Nippon Steel Co., Ltd. Yawata Works (72) Inventor Ryo Watanabe 1-1, Hibahata-cho, Tobata-ku, Kitakyushu, Fukuoka Stock of Nippon Steel F term in Yawata Works (reference) 4K013 AA02 BA02 BA12 CA02 CB09 CF13 DA03 DA08 DA10 DA12 EA01 EA12 EA19 4K070 AA03 AB03 AB07 AB17 AC20 AC23 BD09

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 転炉内の脱炭精錬を行った含クロム溶鋼
に還元剤を添加した後にCO2 発生物質を分割添加し、
スラグ中のクロム酸化物の還元処理を行い、次いで、C
2 発生物質を入れた取鍋内に前記還元処理を行った含
クロム溶鋼を出鋼してから減圧二次脱炭精錬を行うこと
を特徴とする低窒素含クロム溶鋼の製造方法。
1. A CO 2 -generating substance is dividedly added after adding a reducing agent to decarburized and smelted chromium-containing steel in a converter.
The chromium oxide in the slag is reduced, and then C
A method for producing a low-nitrogen chromium-containing molten steel, characterized in that the reduced chromium-containing molten steel is tapped in a ladle containing an O 2 -generating substance, and then depressurized secondary decarburization refining is performed.
【請求項2】 請求項1記載の低窒素含クロム溶鋼の製
造方法において、前記CO2 発生物質を入れた取鍋内の
前記含クロム溶鋼にスラグ低融点化剤を添加することを
特徴とする低窒素含クロム溶鋼の製造方法。
2. The method for producing low nitrogen chromium-containing molten steel according to claim 1, wherein a slag-lowering agent is added to the chromium-containing molten steel in the ladle containing the CO 2 generating substance. Method for producing low nitrogen chromium-containing molten steel.
【請求項3】 請求項1又は2記載の低窒素含クロム溶
鋼の製造方法において、前記CO2 発生物質を炭酸カル
シウムとし、前記スラグ低融点化剤をSiO 2 ・Al2
3 系からなるフラックスを用い、生成したCaO濃度
に対するSiO2 とAl2 3 濃度の比が1.3〜1.
8になるように調整することを特徴とする低窒素含クロ
ム溶鋼の製造方法。
3. The low-nitrogen chromium-containing solution according to claim 1 or 2.
In the method for producing steel, the CO2Generated carbon dioxide
Sium and the slag lowering agent is SiO 2・ Al2
O3Concentration of CaO produced using a flux composed of a system
Against SiO2And Al2O3The concentration ratio is 1.3-1.
Low nitrogen-containing black characterized by adjusting to 8
Method for producing molten steel.
【請求項4】 請求項1〜3のいずれか1項に記載の低
窒素含クロム溶鋼の製造方法において、前記減圧二次脱
炭精錬で前記含クロム溶鋼に昇熱用Al合金を添加する
ことを特徴とする低窒素含クロム溶鋼の製造方法。
4. The method for producing a low nitrogen chromium-containing molten steel according to claim 1, wherein an Al alloy for heating is added to the chromium-containing molten steel in the reduced pressure secondary decarburization refining. A method for producing a low-nitrogen chromium-containing molten steel, characterized by:
【請求項5】 請求項1〜4のいずれか1項に記載の低
窒素含クロム溶鋼の製造方法において、前記CO2 発生
物質が炭酸カルシウムであり、前記減圧二次脱炭精錬で
添加した昇熱用Al合金と反応して生成したCaOとA
2 3 の比が1.2〜1.6となるように調整するこ
とを特徴とする低窒素含クロム溶鋼の製造方法。
5. The method for producing a low nitrogen chromium-containing molten steel according to claim 1, wherein the CO 2 generating substance is calcium carbonate, and the CO 2 generating substance added in the reduced pressure secondary decarburization refining is used. CaO and A produced by reaction with Al alloy for heat
A method for producing a low nitrogen chromium-containing molten steel, which comprises adjusting the ratio of l 2 O 3 to be 1.2 to 1.6.
【請求項6】 請求項1〜5のいずれか1項に記載の低
窒素含クロム溶鋼の製造方法において、前記取鍋の底部
に設けたポーラスプラグの外周囲をアルゴンガス雰囲気
にシールしていることを特徴とする低窒素含クロム溶鋼
の製造方法。
6. The method for producing low nitrogen chromium-containing molten steel according to claim 1, wherein the outer periphery of the porous plug provided at the bottom of the ladle is sealed with an argon gas atmosphere. A method for producing a low-nitrogen chromium-containing molten steel, which is characterized by the above.
JP2002098202A 2002-04-01 2002-04-01 Method for producing low nitrogen-containing chromium molten steel Expired - Fee Related JP3774674B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002098202A JP3774674B2 (en) 2002-04-01 2002-04-01 Method for producing low nitrogen-containing chromium molten steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002098202A JP3774674B2 (en) 2002-04-01 2002-04-01 Method for producing low nitrogen-containing chromium molten steel

Publications (2)

Publication Number Publication Date
JP2003293022A true JP2003293022A (en) 2003-10-15
JP3774674B2 JP3774674B2 (en) 2006-05-17

Family

ID=29240303

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002098202A Expired - Fee Related JP3774674B2 (en) 2002-04-01 2002-04-01 Method for producing low nitrogen-containing chromium molten steel

Country Status (1)

Country Link
JP (1) JP3774674B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011084782A (en) * 2009-10-16 2011-04-28 Jfe Steel Corp Method for producing high chromium steel
JP2013204086A (en) * 2012-03-28 2013-10-07 Nisshin Steel Co Ltd Method for producing stainless steel
JP2016166427A (en) * 2016-06-14 2016-09-15 日新製鋼株式会社 Method for producing stainless steel
WO2020004501A1 (en) * 2018-06-28 2020-01-02 日本製鉄株式会社 Steel manufacturing method

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011084782A (en) * 2009-10-16 2011-04-28 Jfe Steel Corp Method for producing high chromium steel
JP2013204086A (en) * 2012-03-28 2013-10-07 Nisshin Steel Co Ltd Method for producing stainless steel
JP2016166427A (en) * 2016-06-14 2016-09-15 日新製鋼株式会社 Method for producing stainless steel
WO2020004501A1 (en) * 2018-06-28 2020-01-02 日本製鉄株式会社 Steel manufacturing method
KR20200118191A (en) 2018-06-28 2020-10-14 닛폰세이테츠 가부시키가이샤 How to make a lecture

Also Published As

Publication number Publication date
JP3774674B2 (en) 2006-05-17

Similar Documents

Publication Publication Date Title
JP6011728B2 (en) Hot metal dephosphorization method
JP3428628B2 (en) Stainless steel desulfurization refining method
JPS63195209A (en) Steel making method
TWI685577B (en) Smelting method of high manganese steel
JP3774674B2 (en) Method for producing low nitrogen-containing chromium molten steel
JP2006249568A (en) Method for producing molten iron having low phosphorus
US4356032A (en) Method of dephosphorizing molten pig iron
JP3002593B2 (en) Melting method of ultra low carbon steel
EP0043238B1 (en) Method of dephosphorizing molten pig iron
JPH10140227A (en) Production of high alloy steel by joining two molten steels
JP4411934B2 (en) Method for producing low phosphorus hot metal
CN111893247A (en) Steelmaking method with high-efficiency refining function
JP4192503B2 (en) Manufacturing method of molten steel
WO2003029498A1 (en) Method for pretreatment of molten iron and method for refining
JPH0477046B2 (en)
KR102171769B1 (en) Method for processing molten material and stainless steel manufactured using the same
JPH06228626A (en) Method for reforming slag as pretreatment of desulfurization
JP2882236B2 (en) Stainless steel manufacturing method
US4065297A (en) Process for dephosphorizing molten pig iron
JP5544818B2 (en) Melting method of high chromium steel
US6261339B1 (en) Method for desiliconizing pig iron before refining it to steel
JPH0557327B2 (en)
JPH01252715A (en) Method for operating iron bath type smelting reduction furnace
JPH0841519A (en) Steelmaking method
JPS6152208B2 (en)

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20040902

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20051129

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20051213

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060118

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060214

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060220

R151 Written notification of patent or utility model registration

Ref document number: 3774674

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R151

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090224

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100224

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100224

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110224

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110224

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120224

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120224

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130224

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130224

Year of fee payment: 7

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130224

Year of fee payment: 7

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130224

Year of fee payment: 7

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130224

Year of fee payment: 7

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140224

Year of fee payment: 8

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

LAPS Cancellation because of no payment of annual fees